Support radiopharmaceutical manufacturing documentation at Jubilant Radiopharma using GMP awareness, SAP, and meticulous record review. Help protect documentation accuracy across production activities.

As a Production Documentalist, you will coordinate, review, and manage manufacturing documentation with Production, Quality Control, and Quality teams. Your work supports documentation integrity, good documentation practices, compliance, and continuous improvement. The role includes batch records, logbooks, registers, and other GMP-related documents.

Key Responsibilities:

- Coordinate and distribute documentation after manufacturing batch activities
- Print, prepare, verify, and release production documents
- Review and approve batch records and GMP documentation




- Prepare weekly documentation performance KPI reports
- Support document management, archiving, and process improvements

Requirements:

- Experience in pharmaceutical production
- Solid attention to detail and sustained concentration
- Manual dexterity for documentation-related activities
- Proficiency with Microsoft Word, SAP, and Excel
- French and English spoken and written knowledge

Bring pharmaceutical production experience, documentation discipline, and system proficiency to Jubilant Radiopharma’s quality-focused operations.

📌 Pharmaceutical Production Documentation Specialist (Kirkland)
🏢 Jubilant Radiopharma
📍 Kirkland